Kartal, A. Et Al. 2021. Novel compound heterozygous mutations in CLCN1 in a patient with myotonia congenita. NEUROMUSCULAR DISORDERS , vol.31 .

Kartal, A., Yildirim, M., Bektas, O., Ucar, C., & Teber, S., (2021). Novel compound heterozygous mutations in CLCN1 in a patient with myotonia congenita. NEUROMUSCULAR DISORDERS , vol.31.

Kartal, A. Et Al. "Novel compound heterozygous mutations in CLCN1 in a patient with myotonia congenita," NEUROMUSCULAR DISORDERS , vol.31, 2021

Kartal, A. Et Al. "Novel compound heterozygous mutations in CLCN1 in a patient with myotonia congenita." NEUROMUSCULAR DISORDERS , vol.31, 2021

Kartal, A. Et Al. (2021) . "Novel compound heterozygous mutations in CLCN1 in a patient with myotonia congenita." NEUROMUSCULAR DISORDERS , vol.31.

@article{article, author={A. Kartal Et Al. }, title={Novel compound heterozygous mutations in CLCN1 in a patient with myotonia congenita}, journal={NEUROMUSCULAR DISORDERS}, year=2021}